US2923408A - Flotation process - Google Patents
Flotation process Download PDFInfo
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- US2923408A US2923408A US477951A US47795154A US2923408A US 2923408 A US2923408 A US 2923408A US 477951 A US477951 A US 477951A US 47795154 A US47795154 A US 47795154A US 2923408 A US2923408 A US 2923408A
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- ore
- acrylamide
- pulp
- concentrate
- flotation
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- 238000000034 method Methods 0.000 title claims description 18
- 238000005188 flotation Methods 0.000 title claims description 14
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 claims description 42
- 239000012141 concentrate Substances 0.000 claims description 31
- 239000004927 clay Substances 0.000 claims description 25
- 239000001103 potassium chloride Substances 0.000 claims description 21
- 235000011164 potassium chloride Nutrition 0.000 claims description 21
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 12
- 238000009291 froth flotation Methods 0.000 claims description 9
- 229920000642 polymer Polymers 0.000 claims description 9
- 230000001143 conditioned effect Effects 0.000 claims description 8
- 239000000243 solution Substances 0.000 claims description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
- NIXOWILDQLNWCW-UHFFFAOYSA-N Acrylic acid Chemical compound OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 5
- 229920001577 copolymer Polymers 0.000 claims description 5
- 230000003750 conditioning effect Effects 0.000 claims description 4
- 229920001519 homopolymer Polymers 0.000 claims description 4
- 238000002360 preparation method Methods 0.000 claims description 4
- 239000012153 distilled water Substances 0.000 claims description 3
- 238000011084 recovery Methods 0.000 claims description 3
- 229920006395 saturated elastomer Polymers 0.000 claims description 3
- 229920002401 polyacrylamide Polymers 0.000 description 26
- 229910052500 inorganic mineral Inorganic materials 0.000 description 9
- 235000010755 mineral Nutrition 0.000 description 9
- 239000011707 mineral Substances 0.000 description 9
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 9
- 239000003795 chemical substances by application Substances 0.000 description 6
- 239000007864 aqueous solution Substances 0.000 description 5
- 239000012267 brine Substances 0.000 description 5
- 239000002516 radical scavenger Substances 0.000 description 5
- 238000000926 separation method Methods 0.000 description 4
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- 150000001805 chlorine compounds Chemical group 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- LGXVIGDEPROXKC-UHFFFAOYSA-N 1,1-dichloroethene Chemical class ClC(Cl)=C LGXVIGDEPROXKC-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- QTWJRLJHJPIABL-UHFFFAOYSA-N 2-methylphenol;3-methylphenol;4-methylphenol Chemical compound CC1=CC=C(O)C=C1.CC1=CC=CC(O)=C1.CC1=CC=CC=C1O QTWJRLJHJPIABL-UHFFFAOYSA-N 0.000 description 1
- WVYWICLMDOOCFB-UHFFFAOYSA-N 4-methyl-2-pentanol Chemical compound CC(C)CC(C)O WVYWICLMDOOCFB-UHFFFAOYSA-N 0.000 description 1
- CONKBQPVFMXDOV-QHCPKHFHSA-N 6-[(5S)-5-[[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]methyl]-2-oxo-1,3-oxazolidin-3-yl]-3H-1,3-benzoxazol-2-one Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)C[C@H]1CN(C(O1)=O)C1=CC2=C(NC(O2)=O)C=C1 CONKBQPVFMXDOV-QHCPKHFHSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
- 238000006957 Michael reaction Methods 0.000 description 1
- 238000005273 aeration Methods 0.000 description 1
- 238000004220 aggregation Methods 0.000 description 1
- 230000002776 aggregation Effects 0.000 description 1
- 125000005907 alkyl ester group Chemical group 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- -1 aluminum ions Chemical class 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 238000003556 assay Methods 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000002734 clay mineral Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 238000010908 decantation Methods 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 239000008396 flotation agent Substances 0.000 description 1
- 229920006158 high molecular weight polymer Polymers 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- 125000005395 methacrylic acid group Chemical class 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 229920000867 polyelectrolyte Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 238000004064 recycling Methods 0.000 description 1
- 238000009877 rendering Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B03—SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03D—FLOTATION; DIFFERENTIAL SEDIMENTATION
- B03D1/00—Flotation
- B03D1/001—Flotation agents
- B03D1/004—Organic compounds
- B03D1/016—Macromolecular compounds
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B03—SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03D—FLOTATION; DIFFERENTIAL SEDIMENTATION
- B03D1/00—Flotation
- B03D1/001—Flotation agents
- B03D1/004—Organic compounds
- B03D1/01—Organic compounds containing nitrogen
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B03—SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03D—FLOTATION; DIFFERENTIAL SEDIMENTATION
- B03D2201/00—Specified effects produced by the flotation agents
- B03D2201/02—Collectors
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B03—SEPARATION OF SOLID MATERIALS USING LIQUIDS OR USING PNEUMATIC TABLES OR JIGS; MAGNETIC OR ELECTROSTATIC SEPARATION OF SOLID MATERIALS FROM SOLID MATERIALS OR FLUIDS; SEPARATION BY HIGH-VOLTAGE ELECTRIC FIELDS
- B03D—FLOTATION; DIFFERENTIAL SEDIMENTATION
- B03D2203/00—Specified materials treated by the flotation agents; Specified applications
- B03D2203/02—Ores
- B03D2203/04—Non-sulfide ores
- B03D2203/10—Potassium ores
Definitions
- This invention relates to a method for the separation of minerals and is particularly directed to a method for separating clays from other minerals by selective flotaa a particular problem in the beneficiation of sylvinite ores, -such as those found in the Carlsbad district of New Mexico.
- the latter ores. are beneficiated by suspending the finely ground ore in a brine to form a the potassium chloride from the other constituents of the ore by flotation.
- clay slimes have proved particularly troublesome, since such slimes have the undesirable characteristic of sorbing relatively large quantities of flotation agents, thus rendering them inactive.
- high molecular weight polymers of acrylamide are effective collectors for clay in froth-flotation processes. It is among the advantages of the invention that the acrylamide polymers have selective collector activity, whereby clays may be separated from other minerals by flotation.
- the effective acrylamide polymers are water-soluble and characterized by a relatively small degree of crosslinking. 'centipoise for a 0.5 percent by weight solution of the They have a viscosity of at least about one polymer in distilled water adjusted to a pH of 3 to 3.5 and a temperature of 21.5 C.
- the term viscosity as hereinafter employed refers to the viscosity of a 0.5 percent solution of acrylamide polymer under the above conditions as measured with an Ostwald viscosimeter.
- acrylamide polymer includes not only the homopolymers of acrylamide but also co-polymers of acrylamide with up to 15 mole percent of other suitable mono mers, such as methacrylamide, acrylic and methacrylic acids and the lower alkyl esters thereof, acrylonitrile, vinyl and vinylidene chlorides and the like, providedeach such co-polymer is characterized by water solubility and viscosity properties. as set forth above.
- the ore is ground and suspended in an aqueous medium to release the clayminerals in finely divided form.
- the resulting suspension of mineral solids is admixed with a dilute aqueous solution of an effective acrylamide polymer and the resulting mixture is submitted to froth flotation in conventional fashion.
- a frothing agent and in general, good rlll$ have been obtained
- aqueous solutions of the acrylamide polymer In the preparation of aqueous solutions of the acrylamide polymer, the latter is mixed with water or an aqueous solution of soluble constituentsof the ore to be treated, while the mixture is agitated vigorously, conveniently at room temperature.
- the acrylamide polymer may be employed in the dried flake or powdered form or the highly viscous concentrated aqueous compositions obtained by aqueous polymerization of acrylamide may be used directly.
- the dilute aqueous solutions of acrylamide polymer may contain from about 0.003 to about 0.5 percent by weight of polymer.
- aconcentrate consisting of an aqueous solution containing from about 1 to 5 percent by weight of the acrylamide polymer and to dilute this concentrate as needed to obtain the dilute aqueous treating solution.
- water containing a minimum of polyvalent metal ions, such as ferric and aluminum ions since such ions may render the concentrates gel-like and difficult to handle.
- the amount of acrylamide polymer to bev employed will vary depending upon such factors asthe percentage of clay in the pulp, the type of clay and the degree of subdivision of the minerals. In general, from about 0.03 to about 1 pound of the polymer is employed per ton of ore solids. Increased proportions of the acrylamide'polymer collector may sometimes be required as, for example, in the floating of ceramic clays or in the treatment of ores containing a high proportion of clay.
- the present invention has been found particularly useful in the beneficiation of sylvinite ores.
- a froth-flotation process employing an acrylamide polymer as a collector for separating a clay concentrate prior to the floating of potassium chloride from sylvinite ores constitutes a preferred embodiment of the inevntion.
- the pulp was then conditioned for a period of'about l5'seconds with polypropylene glycol methyl ether (Dowfroth 250) at the rate of 0.16 pound perton of ore and submitted to froth flotation. A clay concentrate was separated fora period of 4 minutes. The remaining pulp was then conditioned with along chain aliphatic amine acetate (Armac TD) at the rate of 0.5 pound per ton of ore and postassium chloride-bearing froth separated for 3 minutes.
- TD chain aliphatic amine acetate
- results are set forth in the following table, together with heldundisturbed for a short period of tim'e to allow "most of the salt crystals to settle.
- the supernatant liquid con.- taining suspended clay was then decanted. These washing and decanting steps were repeated twice more with .250 milliliter portions of the brine and, the three portions of decanted slimes were combinedv and assayed as clay concentrate.
- the washed crystal pulp was transferredto the flotation machine with suflicient brine to fill the cell.
- Example 2 Further samples of the sylvinite ore prepared as in Example 1 were conditioned with acrylamide polymers of varying viscosities. The frothing agent and flotation techniques employed were as in Example 1 except that the acrylamide polymer was added. in one-half minute and the frothing time for the potassium chloride concentrate was from 2 to 3 minutes, in which time it appeared that the separation of potassium chloride was essentially complete. The amount and viscosity of acrylamide polymer,
- Example 2 Further determinations were carried out following the procedure of Example 2 employing 0.22 pound of the UIOOOON acrylamide polymer of Example 1 per ton of ore. These determinations were designed to demonstrate the applicability of other frothing agents. The results obtained were as follows:
- Sylvinite ore pulp prepared as in Example 1 was conditioned with 0.6 pound of the acrylamide polymer of Example 1 per ton of ore anda clay concentrate floated off following the technique and employing the frothing agent of Example 1.. Thereafter, Armac TD was added to the pulp at the rate of 025 pound per ton of ore and a potassi um chloride-bearing froth was separated for.3 minutes.
- the percentage distribution of potassium chloride was as follows: Clay concentrate 2.7 percent, potassium chloride concentrate, 86,5 percent; and tails 10.8 percent.
- the potassium chloride concentrate assayed 81 percent KCl.
- the acrylamide polymer of the present invention demonstrates selective collector activity for clay, whereby the clay concentrate carries with it considerably less potassium chloride than is lost in the decantation procedure.
- the loss of potassium chloridevalues in the clay concentrate is particularlyunclesirable'in that little can be done in the way of recoveringthe yaluesfrom the clay concentrate except by expensive thermal methods. Values left-in the. tails, on the other hand, can be recovered by a scavenger flotation, as shown, for example, byythe following determinations.
- Example 5 1 A solution of 0.0275 gram of the acrylamide polymer of Example 1 in 100 milliliters of saturated brine prepared from sylvinite ore was added in 3 approximately equal portions with stirring during a period of 0.5 minute to a pulp containing 250 grams of sylvinite ore prepared as in Example 1. The above treatnient resulted in the introductioninto the pulp of. acrylamide polymer at the rateof 0.22 pound per ton of ore. The treated pulpwas transferred to the flotation machine, brought to volume as in the preceding examples and conditioned for a period of about 15 seconds with 0.16 pound of Dowfroth 250 per ton of ore. Aeration was then begun and a 'clay concentrate was separated for a period of about 4 minutes.
- a method which comprises the successive stepsof suspending ground sylvinite ore in brine saturated with respect thereto, conditioning the resulting pulp with a frothing agent and a water-soluble acrylamide polymer characterized by a viscosity of from 1.8 to 80 centiposes V for a 0.5 percent solution thereof indistilledlwater adjus'ted to a pH of3 to 3.5 anda temperature of 2 5.
- C
- the polymer employed being selected from the group consisting of homopolymers of acrylamide and copolymers of acrylamide with up to 15 mole percent of acrylic acid.
Landscapes
- Separation Of Suspended Particles By Flocculating Agents (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Paper (AREA)
Description
-pulp and separating Uni-ted States Patent 2,923,408 FLOTATION PROCESS Carl F. Williams, Pleasant Hill, Calif., assignor to The Dow Chemical Company,.Midland, M1ch., a corporation of Delaware No Drawing. Application December 27, 1954 Serial No. 477,951
3 Claims. (Cl. 209-166) This invention relates to a method for the separation of minerals and is particularly directed to a method for separating clays from other minerals by selective flotaa a particular problem in the beneficiation of sylvinite ores, -such as those found in the Carlsbad district of New Mexico. In general, the latter ores. are beneficiated by suspending the finely ground ore in a brine to form a the potassium chloride from the other constituents of the ore by flotation. In such operations, as pointed out, for example, in US. Patents 2,364,520 and 2,569,672, clay slimes have proved particularly troublesome, since such slimes have the undesirable characteristic of sorbing relatively large quantities of flotation agents, thus rendering them inactive.
It is an object of the present invention to provide an improved method for separating clay and clay-like minerals from ores. for selectively separating clay from other minerals by froth-flotation. Another object is to provide a process for the beneficiation of sylvinite ore, wherein said ore is deslimed by flotation. Other objects will become apparent from the following specification and claims.
According to the present invention it has been discovered that high molecular weight polymers of acrylamide are effective collectors for clay in froth-flotation processes. It is among the advantages of the invention that the acrylamide polymers have selective collector activity, whereby clays may be separated from other minerals by flotation.
The effective acrylamide polymers are water-soluble and characterized by a relatively small degree of crosslinking. 'centipoise for a 0.5 percent by weight solution of the They have a viscosity of at least about one polymer in distilled water adjusted to a pH of 3 to 3.5 and a temperature of 21.5 C. The term viscosity as hereinafter employed refers to the viscosity of a 0.5 percent solution of acrylamide polymer under the above conditions as measured with an Ostwald viscosimeter. The
term acrylamide polymer includes not only the homopolymers of acrylamide but also co-polymers of acrylamide with up to 15 mole percent of other suitable mono mers, such as methacrylamide, acrylic and methacrylic acids and the lower alkyl esters thereof, acrylonitrile, vinyl and vinylidene chlorides and the like, providedeach such co-polymer is characterized by water solubility and viscosity properties. as set forth above.
In carrying out the invention, the ore is ground and suspended in an aqueous medium to release the clayminerals in finely divided form. The resulting suspension of mineral solids is admixed with a dilute aqueous solution of an effective acrylamide polymer and the resulting mixture is submitted to froth flotation in conventional fashion. In such operations, it is usual to employ a frothing agent and in general, good rlll$ have been obtained It is a further object to provide a method by use of frothing agents free of specific collector activity, such as, for example, cresylic acid, methyl isobutyl carbinol or the propylene glycol monoethers described in US. Patent 2,611,485.
In the preparation of aqueous solutions of the acrylamide polymer, the latter is mixed with water or an aqueous solution of soluble constituentsof the ore to be treated, while the mixture is agitated vigorously, conveniently at room temperature. In such preparations, the acrylamide polymer may be employed in the dried flake or powdered form or the highly viscous concentrated aqueous compositions obtained by aqueous polymerization of acrylamide may be used directly. For direct application in mineral pulps, the dilute aqueous solutions of acrylamide polymer may contain from about 0.003 to about 0.5 percent by weight of polymer. In mill practice, it is convenient to prepare aconcentrate consisting of an aqueous solution containing from about 1 to 5 percent by weight of the acrylamide polymer and to dilute this concentrate as needed to obtain the dilute aqueous treating solution. In preparing such concentrates it is preferred to employ water containing a minimum of polyvalent metal ions, such as ferric and aluminum ions, since such ions may render the concentrates gel-like and difficult to handle.
The amount of acrylamide polymer to bev employed will vary depending upon such factors asthe percentage of clay in the pulp, the type of clay and the degree of subdivision of the minerals. In general, from about 0.03 to about 1 pound of the polymer is employed per ton of ore solids. Increased proportions of the acrylamide'polymer collector may sometimes be required as, for example, in the floating of ceramic clays or in the treatment of ores containing a high proportion of clay.
The present invention has been found particularly useful in the beneficiation of sylvinite ores. A froth-flotation process employing an acrylamide polymer as a collector for separating a clay concentrate prior to the floating of potassium chloride from sylvinite ores constitutes a preferred embodiment of the inevntion.
The following examples illustrate the inventionbut are not to be construed as limiting the same.
posits in the Carlsbad, NewMexico, region and containing about 26 percent KCl, was ground to pass a 28 mesh screen and suspended in 250 milliliters of saturated brine prepared from the same ore. To the resulting pulp, a solution of 0.0375 gram of acrylamide polymer in milliliters of the saturated brine was added portionwise with stirring during a period of about one minute. The polymer employed had a viscosity of 7 centipoises. The above treatment resulted in the introduction of acrylamide polymer at the ,rate of 0.3 poundper ton of ore. The treated pulp was transferred to a 950 milliliter minerals separation subaeration type flotation machine and additional saturated brine added to fill the machine. The pulp was then conditioned for a period of'about l5'seconds with polypropylene glycol methyl ether (Dowfroth 250) at the rate of 0.16 pound perton of ore and submitted to froth flotation. A clay concentrate was separated fora period of 4 minutes. The remaining pulp was then conditioned with along chain aliphatic amine acetate (Armac TD) at the rate of 0.5 pound per ton of ore and postassium chloride-bearing froth separated for 3 minutes. The
results are set forth in the following table, together with heldundisturbed for a short period of tim'e to allow "most of the salt crystals to settle. The supernatant liquid con.- taining suspended clay was then decanted. These washing and decanting steps were repeated twice more with .250 milliliter portions of the brine and, the three portions of decanted slimes were combinedv and assayed as clay concentrate. The washed crystal pulp was transferredto the flotation machine with suflicient brine to fill the cell.
Armac TD (0.5 pound per ton) and Dowfroth 250 (0.16
pound per ton) were added and the flotation of a potassium chloride concentrate carried outas before. In the table the results are summarized in terms of the assay of the potassium chloride (KCl) concentrate and the percent of the total potassium chloride recovered in the clay concentrate, potassium chloride concentrate and tailings.
Percent by Percent of Available K01 Wei ht of Recovered in- Acrylamlde Polymer, KCl in Pounds/ton K01 Concentrate Clay K01 Tails Cone. Cone.
0.30 84.4 4.0 83.6 12.4 None 81.0 18. 1 75. 3 6. 6
Example 2 Further samples of the sylvinite ore prepared as in Example 1 were conditioned with acrylamide polymers of varying viscosities. The frothing agent and flotation techniques employed were as in Example 1 except that the acrylamide polymer was added. in one-half minute and the frothing time for the potassium chloride concentrate was from 2 to 3 minutes, in which time it appeared that the separation of potassium chloride was essentially complete. The amount and viscosity of acrylamide polymer,
frothing times for the clay concentrate and results of the separations are summarized in the following table:
Further determinations were carried out following the procedure of Example 2 employing 0.22 pound of the UIOOOON acrylamide polymer of Example 1 per ton of ore. These determinations were designed to demonstrate the applicability of other frothing agents. The results obtained were as follows:
Sylvinite ore pulp prepared as in Example 1 was conditioned with 0.6 pound of the acrylamide polymer of Example 1 per ton of ore anda clay concentrate floated off following the technique and employing the frothing agent of Example 1.. Thereafter, Armac TD was added to the pulp at the rate of 025 pound per ton of ore and a potassi um chloride-bearing froth was separated for.3 minutes.
The percentage distribution of potassium chloride was as follows: Clay concentrate 2.7 percent, potassium chloride concentrate, 86,5 percent; and tails 10.8 percent. The potassium chloride concentrate assayed 81 percent KCl.
In the above examples it will be noted that the acrylamide polymer of the present invention demonstrates selective collector activity for clay, whereby the clay concentrate carries with it considerably less potassium chloride than is lost in the decantation procedure. The loss of potassium chloridevalues in the clay concentrate is particularlyunclesirable'in that little can be done in the way of recoveringthe yaluesfrom the clay concentrate except by expensive thermal methods. Values left-in the. tails, on the other hand, can be recovered by a scavenger flotation, as shown, for example, byythe following determinations.
. Example 5 1 A solution of 0.0275 gram of the acrylamide polymer of Example 1 in 100 milliliters of saturated brine prepared from sylvinite ore was added in 3 approximately equal portions with stirring during a period of 0.5 minute to a pulp containing 250 grams of sylvinite ore prepared as in Example 1. The above treatnient resulted in the introductioninto the pulp of. acrylamide polymer at the rateof 0.22 pound per ton of ore. The treated pulpwas transferred to the flotation machine, brought to volume as in the preceding examples and conditioned for a period of about 15 seconds with 0.16 pound of Dowfroth 250 per ton of ore. Aeration was then begun and a 'clay concentrate was separated for a period of about 4 minutes. Thereafter the pulp was conditioned with 'Armac TD at the rate of 0.5 pound per ton of ore and 1 a rougher concentrate of potassium chloride was separated. The remaining pulp, corresp ding to the tails of the preceding examples, was then subjected to two further froth flotations with additional Armac TD atthe rate of 0.5 pound per ton before eachfiotation period to separate first and second scavenger concentrates. The results are summarized in the following table:
Percent by ,Percent of Wei ht K01 Re- KCl covered Heads (E'uployefl as Cell Fee 26. 2 100 Clay Concentrate 3. Rougher Concentrate- V 84. 9 81. First scavenger concentrate 52. 8 9.
' Second scavenger concentrate. 24. 7 2. Tails 1.3 3.
It will be noted that the recovery of potassium chloride in the rougher and scavenger stages of flotation totaled 93.3 percent and thescavenger concentrates were .er
suitable grade for recycling to the rougher cell.
I claim: v I m V 1. In the preparation of sylvinite ore for the recovery of potassium chlorideby flotation, the method which comprises the steps of suspending ground sylvinite die in brine saturated with respect to said ore to form a pulp, conditioning said pulp with a frotherandwith a water-soluble acrylamide polymer characterized by a viscosity of from 1.8 to centiposes for a 0.5 percent by weight solution thereof in distilled water adjusted to a pH of 3 to 3.5 and at a temperatureof 21.5 0., subjecting the conditioned pulp to froth flotation and separating clay therefrom as aflotated concentrate, the polymer employed being selected from the group consisting of homopolymers of acrylamide and copolymers of acrylamide with up to 15 mole. percent of acrylic acid.
2. A method which comprises the successive stepsof suspending ground sylvinite ore in brine saturated with respect thereto, conditioning the resulting pulp with a frothing agent and a water-soluble acrylamide polymer characterized by a viscosity of from 1.8 to 80 centiposes V for a 0.5 percent solution thereof indistilledlwater adjus'ted to a pH of3 to 3.5 anda temperature of 2 5. C;
as a fiotated clay concentrate, conditioning the remaining pulp with a potassium chloride collector and recovering a crystalline potassium chloride concentrate from the pulp by froth flotation, the polymer employed being selected from the group consisting of homopolymers of acrylamide and copolymers of acrylamide with up to 15 mole percent of acrylic acid.
3. A method according to claim 1, wherein the acrylamide polymer is employed in the amount of from about 0.03 to about 1 pound per ton of ore.
References Cited in the file of this patent UNITED STATES PATENTS Ogilley Apr. 25, 1944 15 6 7 Jackson Oct. 2, 1951 Jones Nov. 16, 1954 Atwood et a1. Dec. 14, 1954 Aimone et a1. Apr. 3, 1956 FOREIGN PATENTS Australia Jan. 19, 1954 OTHER REFERENCES Michaels: Aggregation of Suspensions by Polyelectrolytes, Industrial and Engineering Chemistry, July 1954, pages 1485-1490.
Claims (1)
1. IN THE PREPARATION OF SYLVINITE ORE FOR THE RECOVERY OF POTASSIUM CHLORIDE BY FLOTATION, THE METHOD WHICH COMPRISES THE STEPS OF SUSPENDING GROUND SYLVINITE ORE IN BRINE SATURATED WITH RESPECT TO SAID ORE TO FORM A PULP, CONDITIONING SAID PULP WITH A FROTHER AND WITH A WATER-SOLUBLE ACRYLAMIDE POYMER CHARACTERIZED BY A VISCOSITY OF FROM 1.8 TO 80 CENTIPOSES FOR A 0.5 PERCENT BY WEIGHT SOLUTION THEREOF IN DISTILLED WATER ADJUSTED TO A PH OF 3 TO 3.5 AND AT A TEMPERATURE OF 21.5*C., SUBJECTING THE CONDITIONED PULP TO FROTH FLOTATION AND SEPARATING CLAY THEREFROM AS A FLOTATED CONCENTRATE, THE POLYMER EMPOLYED BEING SELECTED FROM THE GROUP CONSISTING OF HOMOPOLYMERS OF ACRYLAMIDE AND COPOLYMERS OF ACRYLAMIDE WITH UP TO 15 MOLE PERCENT OF ACRYLIC ACID.
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US477951A US2923408A (en) | 1954-12-27 | 1954-12-27 | Flotation process |
| FR1139954D FR1139954A (en) | 1954-12-27 | 1955-12-20 | Process improvements for mineral separation |
| DED21989A DE1054392B (en) | 1954-12-27 | 1955-12-23 | Separation of clay by flotation from clay-containing mineral solids |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US477951A US2923408A (en) | 1954-12-27 | 1954-12-27 | Flotation process |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2923408A true US2923408A (en) | 1960-02-02 |
Family
ID=23897973
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US477951A Expired - Lifetime US2923408A (en) | 1954-12-27 | 1954-12-27 | Flotation process |
Country Status (3)
| Country | Link |
|---|---|
| US (1) | US2923408A (en) |
| DE (1) | DE1054392B (en) |
| FR (1) | FR1139954A (en) |
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3138550A (en) * | 1960-11-28 | 1964-06-23 | Union Carbide Corp | Froth flotation process employing polymeric flocculants |
| US3259237A (en) * | 1963-04-22 | 1966-07-05 | Saskatchewan Potash | Phase desliming and concentration of potash ores |
| US3452867A (en) * | 1967-03-30 | 1969-07-01 | Hercules Inc | Treatment of sylvinite ores |
| US3545941A (en) * | 1969-03-19 | 1970-12-08 | United States Borax Chem | Settling of hematite slimes |
| US3782546A (en) * | 1971-12-03 | 1974-01-01 | Calgon Corp | Cationic conditioning agents for potash flotation |
| US3805951A (en) * | 1972-04-07 | 1974-04-23 | American Cyanamid Co | Selective flocculation and flotation of slimes from sylvinite ores |
| US4192737A (en) * | 1978-09-15 | 1980-03-11 | The United States Of America As Represented By The Secretary Of The Interior | Froth flotation of insoluble slimes from sylvinite ores |
| DE2649708C3 (en) | 1975-11-03 | 1980-04-10 | Fluor Utah, Inc., San Mateo, Calif. (V.St.A.) | Process for processing potash salts |
| US4198288A (en) * | 1979-03-22 | 1980-04-15 | Celanese Polymer Specialties Company | Desliming of potash ores |
| US4441993A (en) * | 1975-11-03 | 1984-04-10 | Fluor Corporation | Flotation process |
| WO2010097166A1 (en) * | 2009-02-24 | 2010-09-02 | Clariant International Ltd | Collecting agent and method for floatation of insoluble components of raw salts |
| US20110290704A1 (en) * | 2009-02-24 | 2011-12-01 | Clariant Finance (Bvi) Limited | Foaming Agent And Method For Floatation Of Insoluble Components Of Raw Salts |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1254592B (en) * | 1961-09-05 | 1967-11-23 | Dow Chemical Co | Process to improve the filterability of aqueous organic slimes |
| GB1186906A (en) * | 1966-05-11 | 1970-04-08 | Prod Chim D Auby Soc D | Improvements in and relating to the Flotation of Minerals and Ores with a Calcareous and/or Dolomitic Gangue |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2347576A (en) * | 1941-06-21 | 1944-04-25 | Us Rubber Co | Crude rubber |
| US2569672A (en) * | 1950-04-06 | 1951-10-02 | Int Minerals & Chem Corp | Flotation of slimes from sylvinite ore with hydroxyethyl cellulose |
| US2694702A (en) * | 1951-04-13 | 1954-11-16 | Dow Chemical Co | Soluble chloromethylated polymers of styrene and alpha-methyl styrene, their quaternary ammonium salts and method of making the same |
| US2696912A (en) * | 1953-02-02 | 1954-12-14 | Duval Sulphur & Potash Company | Concentrating or separating of the values from soluble ores |
| US2740522A (en) * | 1953-04-07 | 1956-04-03 | American Cyanamid Co | Flotation of ores using addition polymers as depressants |
-
1954
- 1954-12-27 US US477951A patent/US2923408A/en not_active Expired - Lifetime
-
1955
- 1955-12-20 FR FR1139954D patent/FR1139954A/en not_active Expired
- 1955-12-23 DE DED21989A patent/DE1054392B/en active Pending
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2347576A (en) * | 1941-06-21 | 1944-04-25 | Us Rubber Co | Crude rubber |
| US2569672A (en) * | 1950-04-06 | 1951-10-02 | Int Minerals & Chem Corp | Flotation of slimes from sylvinite ore with hydroxyethyl cellulose |
| US2694702A (en) * | 1951-04-13 | 1954-11-16 | Dow Chemical Co | Soluble chloromethylated polymers of styrene and alpha-methyl styrene, their quaternary ammonium salts and method of making the same |
| US2696912A (en) * | 1953-02-02 | 1954-12-14 | Duval Sulphur & Potash Company | Concentrating or separating of the values from soluble ores |
| US2740522A (en) * | 1953-04-07 | 1956-04-03 | American Cyanamid Co | Flotation of ores using addition polymers as depressants |
Cited By (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3138550A (en) * | 1960-11-28 | 1964-06-23 | Union Carbide Corp | Froth flotation process employing polymeric flocculants |
| US3259237A (en) * | 1963-04-22 | 1966-07-05 | Saskatchewan Potash | Phase desliming and concentration of potash ores |
| US3452867A (en) * | 1967-03-30 | 1969-07-01 | Hercules Inc | Treatment of sylvinite ores |
| US3545941A (en) * | 1969-03-19 | 1970-12-08 | United States Borax Chem | Settling of hematite slimes |
| US3782546A (en) * | 1971-12-03 | 1974-01-01 | Calgon Corp | Cationic conditioning agents for potash flotation |
| US3805951A (en) * | 1972-04-07 | 1974-04-23 | American Cyanamid Co | Selective flocculation and flotation of slimes from sylvinite ores |
| US4441993A (en) * | 1975-11-03 | 1984-04-10 | Fluor Corporation | Flotation process |
| DE2649708C3 (en) | 1975-11-03 | 1980-04-10 | Fluor Utah, Inc., San Mateo, Calif. (V.St.A.) | Process for processing potash salts |
| DE2660423C2 (en) * | 1975-11-03 | 1981-10-01 | Fluor Utah, Inc., San Mateo, Calif. | Process for processing uranium ores |
| DE2660422C2 (en) * | 1975-11-03 | 1981-10-01 | Fluor Utah, Inc., San Mateo, Calif. | Process for the preparation of copper salts |
| US4192737A (en) * | 1978-09-15 | 1980-03-11 | The United States Of America As Represented By The Secretary Of The Interior | Froth flotation of insoluble slimes from sylvinite ores |
| US4198288A (en) * | 1979-03-22 | 1980-04-15 | Celanese Polymer Specialties Company | Desliming of potash ores |
| WO2010097166A1 (en) * | 2009-02-24 | 2010-09-02 | Clariant International Ltd | Collecting agent and method for floatation of insoluble components of raw salts |
| US20110290704A1 (en) * | 2009-02-24 | 2011-12-01 | Clariant Finance (Bvi) Limited | Foaming Agent And Method For Floatation Of Insoluble Components Of Raw Salts |
| US20110290705A1 (en) * | 2009-02-24 | 2011-12-01 | Clariant Finance (Bvi) Limited | Collecting Agent and Method for Floatation of Insoluble Components of Raw Salts |
| US8496115B2 (en) * | 2009-02-24 | 2013-07-30 | Clariant Finance (Bvi) Limited | Foaming agent and method for floatation of insoluble components of raw salts |
| US8534464B2 (en) * | 2009-02-24 | 2013-09-17 | Clariant Finance (Bvi) Limited | Collecting agent and method for floatation of insoluble components of raw salts |
Also Published As
| Publication number | Publication date |
|---|---|
| DE1054392B (en) | 1959-04-09 |
| FR1139954A (en) | 1957-07-09 |
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